Medical Device Recall: Medline medical convenience kits, containing Namic Manifold, Labeled as: 1. ANGIOGRAPHY CATH LAB, Medline Kit Number/SKUDYNJ23532C; 2. CATH LAB PACK, Medline Kit Number/SKUDYNJ65185; 3. ANGIO K
Medline Industries, LP · March 24, 2026
Reason for Recall
Medline has identified the presence of particulate within the fluid path of the Manifolds.
Product Description
Medline medical convenience kits, containing Namic Manifold, Labeled as: 1. ANGIOGRAPHY CATH LAB, Medline Kit Number/SKUDYNJ23532C; 2. CATH LAB PACK, Medline Kit Number/SKUDYNJ65185; 3. ANGIO KIT, Medline Kit Number/SKUVASC1057.
Distribution
US (nationwide) and AE, AU, CA, JP, KR, NL, SG, SK.
States Affected
NATIONWIDE
Quantity Affected
508 kits
Source: FDA (openFDA Device Enforcement)
Recall number: Z-2143-2026
Status: ongoing
SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.